Madame Camille DION / PhD

enseignant-chercheur, enseignant du supérieur*chercheur en milieu académique*médiation scientifique, communication et journalisme scientifique, édition scientifique, relations internationales*

Contact details

camille.dion@univ-amu.fr

Professional contact details

, ,

Jobs

Research : NON

PhD

Title : Pathologie Humaine - Spécialité Génétique humaine

First registration date : 1 October 2014 / 4A

Doctoral school : Sciences de la Vie et de la Santé

Thesis defense date : 18 May 2018

Subject : dynamiques épigénétiques du macrosatellite D4Z4 par la protéine smchd1 dans deux maladies rares : exploitation du modèle ips

Thesis supervisor : MAGDINIER Frédérique

Thesis co-supervisor :

Research unit : MMG - Marseille Medical Genetics

Team : Epigénétique, chromatine et pathologies.

Master's degree

Title : Sciences de la Santé à finalité Recherche, mention Pathologie Humaine

July 2014 - AMU

Mention : Bien

Publications

  • DNA methylation and muscular differentiation of FSHD human induced pluripotent stem cells (hiPSC)
    congrès myologie Lyon 2016, 2016
    Camille Dion, Chérif Badja, Marie-Cécile Gaillard, Claire El-Yazidi, Karine N'Guyen, Stéphane Roche, Frédérique Magdinier

  • Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers
    Neurology, 2014
    Gaillard MC, Roche S, Dion C, Tasmadjian A, Bouget G, Salort-Campana E, Vovan C, Chaix C, Broucqsault N, Morere J, Puppo F, Bartoli M, Levy N, Bernard R, Attarian S, Nguyen K, Magdinier F.

  • De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
    Nature Genetics, 2017
    Christopher T Gordon1,2,40, Shifeng Xue3,4,40, Gökhan Yigit5,40, Hicham Filali1,2,6,40, Kelan Chen7,8,40, Nadine Rosin5, Koh-ichiro Yoshiura9, Myriam Oufadem1,2, Tamara J Beck7, Ruth McGowan10, Alex C Magee11, Janine Altmüller12–14, Camille Dion15, Holger Thiele12, Alexandra D Gurzau7,8, Peter Nürnberg12,14,16, Dieter Meschede17, Wolfgang Mühlbauer18, Nobuhiko Okamoto19, Vinod Varghese20, Rachel Irving20, Sabine Sigaudy21, Denise Williams22, S Faisal Ahmed23, Carine Bonnard3, Mung Kei Kong3, Ilham Ratbi6, Nawfal Fejjal24, Meriem Fikri25, Siham Chafai Elalaoui6,26, Hallvard Reigstad27, Christine Bole-Feysot2,28, Patrick Nitschké2,29, Nicola Ragge22,30, Nicolas Lévy15,21, Gökhan Tunçbilek31, Audrey S M Teo32, Michael L Cunningham33, Abdelaziz Sefiani6,26, Hülya Kayserili34, James M Murphy7,8, Chalermpong Chatdokmaiprai35, Axel M Hillmer32, Duangrurdee Wattanasirichaigoon36, Stanislas Lyonnet1,2,37, Frédérique Magdinier15, Asif Javed32,41, Marnie E Blewitt7,8,41, Jeanne Amiel1,2,37,41, Bernd Wollnik5,13,41 & Bruno Reversade3,4,34,38,39,41

  • Detailed analysis of D4Z4 methylation in FSHD reveals dynamic methylation upon reprogrammingand muscle differentiation
    eLife, 2018
    Stéphane Roche1*, Camille Dion1*, Cherif Badja1, Marie-Cécile Gaillard1, Natacha Broucqsault1, Jérôme D. Robin1, Arnaud Lagarde1;4, Francesca Puppo1, Claire El-Yazidi1, Emilie Barruet1, Julia Morere1, Morgane Thomas1, Emilie Pellier1, Andrée Schlupp Robaglia1;2;3, Catherine Vovan4, Charlene Chaix4, Armand Tasmadjian1, Estelle Balducci1;4, Helene Zattara1;4, Emmanuelle Salort Campana1;5, Shahram Attarian1;5, Bernard Binetruy1;6, Rafaelle Bernard1;4, Marc Bartoli1, Karine Nguyen1;4, Frédérique Magdinier 1#

  • Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report
    BMC Medical Genetics, 2016
    Marie-Cécile Gaillard1†, Francesca Puppo1†, Stéphane Roche1†, Camille Dion1, Emmanuelle Salort Campana1,2, Virginie Mariot3, Charlene Chaix4, Catherine Vovan4, Killian Mazaleyrat1, Armand Tasmadjian1, Rafaelle Bernard1,4, Julie Dumonceaux3, Shahram Attarian1,2, Nicolas Lévy1,4, Karine Nguyen1,4, Frédérique Magdinier1*† and Marc Bartoli1,4†

Languages

Anglais : C1 - Avancé

Français : C2 - Maternel